ClearanceBrief
510(k) K880631 ยท LXJ Interactive Rehabilitation Exercise Devices

2K-QDA MOTION/GAIT ANALYSIS SYSTEM

ApplicantHuman Performance Technologies, Inc., East Setauket NY, US
DecisionSubstantially Equivalent, Apr 21, 1988
ReceivedFeb 16, 1988
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K880631

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.